Canonical Allele Identifier: CA500685925

Linked Data

MyVariant Identifiers: chr17:g.54923059T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56845698T>G , CM000679.2:g.56845698T>G GRCh38
NC_000017.10:g.54923059T>G , CM000679.1:g.54923059T>G GRCh37
NC_000017.9:g.52278058T>G NCBI36
NG_033888.1:g.16600T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000284061.8:c.633T>G (DGKE) MANE Select ENSP00000284061.3:p.Ser211=
ENST00000648772.1:c.*314-1908A>C (TRIM25) ENSP00000498158.1:n.*314-1908A>C
ENST00000284061.7:c.633T>G (DGKE) ENSP00000284061.3:p.Ser211=
ENST00000571084.1:n.169T>G (DGKE)
ENST00000572944.1:c.463T>G (DGKE)
ENST00000576869.5:n.781T>G (DGKE)
NM_003647.2:c.633T>G (DGKE) NP_003638.1:p.Ser211=
XM_011525394.1:c.687T>G (DGKE) XP_011523696.1:p.Ser229=
XM_011525395.1:c.687T>G (DGKE) XP_011523697.1:p.Ser229=
XM_011525396.1:c.687T>G (DGKE) XP_011523698.1:p.Ser229=
XM_011525397.1:c.687T>G (DGKE) XP_011523699.1:p.Ser229=
XM_011525398.1:c.177T>G (DGKE) XP_011523700.1:p.Ser59=
XR_934581.1:n.786T>G (DGKE)
XM_011525394.3:c.687T>G (DGKE) XP_011523696.1:p.Ser229=
XM_011525395.2:c.687T>G (DGKE) XP_011523697.1:p.Ser229=
XM_011525396.2:c.687T>G (DGKE) XP_011523698.1:p.Ser229=
XM_017025243.2:c.633T>G (DGKE) XP_016880732.1:p.Ser211=
XM_017025244.2:c.687T>G (DGKE) XP_016880733.1:p.Ser229=
XR_001752670.2:n.819T>G (DGKE)
XR_001752671.1:n.798T>G (DGKE)
XR_001752672.1:n.799T>G (DGKE)
XR_002958079.1:n.797T>G (DGKE)
NM_003647.3:c.633T>G (DGKE) MANE Select NP_003638.1:p.Ser211=